Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP316139.RAWsos844Zne46IAGNLp52U3Rn-HalJscsBAPzZSh2r7k130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP316139.RAWsos844Zne46IAGNLp52U3Rn-HalJscsBAPzZSh2r7k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP316139.RAWsos844Zne46IAGNLp52U3Rn-HalJscsBAPzZSh2r7k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP316139.RAWsos844Zne46IAGNLp52U3Rn-HalJscsBAPzZSh2r7k130_provenance.
- NP316139.RAWsos844Zne46IAGNLp52U3Rn-HalJscsBAPzZSh2r7k130_assertion description "[These are the first mutations identified in EP300 for a congenital disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316139.RAWsos844Zne46IAGNLp52U3Rn-HalJscsBAPzZSh2r7k130_provenance.
- NP316139.RAWsos844Zne46IAGNLp52U3Rn-HalJscsBAPzZSh2r7k130_assertion evidence source_evidence_literature NP316139.RAWsos844Zne46IAGNLp52U3Rn-HalJscsBAPzZSh2r7k130_provenance.
- NP316139.RAWsos844Zne46IAGNLp52U3Rn-HalJscsBAPzZSh2r7k130_assertion SIO_000772 15706485 NP316139.RAWsos844Zne46IAGNLp52U3Rn-HalJscsBAPzZSh2r7k130_provenance.
- NP316139.RAWsos844Zne46IAGNLp52U3Rn-HalJscsBAPzZSh2r7k130_assertion wasDerivedFrom befree-20140225 NP316139.RAWsos844Zne46IAGNLp52U3Rn-HalJscsBAPzZSh2r7k130_provenance.
- NP316139.RAWsos844Zne46IAGNLp52U3Rn-HalJscsBAPzZSh2r7k130_assertion wasGeneratedBy ECO_0000203 NP316139.RAWsos844Zne46IAGNLp52U3Rn-HalJscsBAPzZSh2r7k130_provenance.
- befree-20140225 importedOn "2014-02-25" NP316139.RAWsos844Zne46IAGNLp52U3Rn-HalJscsBAPzZSh2r7k130_provenance.